ascladiol

2(5H)- furanone, 5-(2-hydroxyethylidene)-4-(hydroxymethyl)- (5E)-5-(2- hydroxyethylidene)-4-(hydroxymethyl)furan-2-one PubMed: Biodegradation Mechanisms of Patulin in Candida guilliermondii: An iTRAQ-Based Proteomic Analysis. PubMed: Patulin Degradation by the Biocontrol Yeast Sporobolomyces sp. Is an Inducible Process. PubMed: Patulin transformation products and last intermediates in its biosynthetic pathway, E- and Z-ascladiol, are not toxic to human cells. PubMed: Effects of patulin and ascladiol on porcine intestinal mucosa: An ex vivo approach. PubMed: Transcriptomic responses of the basidiomycete yeast Sporobolomyces sp. to the mycotoxin patulin. PubMed: Patulin biodegradation by marine yeast Kodameae ohmeri. PubMed: Searching for genes responsible for patulin degradation in a biocontrol yeast provides insight into the basis for resistance to this mycotoxin. PubMed: Divergent synthesis of the co-isolated mycotoxins longianone, isopatulin, and (Z)-ascladiol via furan oxidation. PubMed: Biotransformation of patulin by Gluconobacter oxydans. PubMed: Fate of patulin in the presence of the yeast Saccharomyces cerevisiae. PubMed: Patulin biosynthesis: enzymatic and nonenzymatic transformations of the mycotoxin (E)-ascladiol.